Water-soluble antimony (V) compounds

ABSTRACT

Disclosed is a method of making a tri- or tetrahydrocarbylammonium hexahydroxyantimonate, 
     
         [R.sub.3 R&#39;N]Sb(OH).sub.6 ·xH.sub.2 O             (1) 
    
     containing 3 to 30 C atoms, which process comprises the steps of (1) contacting a compound selected from 
     
         R.sub.3 N and R.sub.4 NOH 
    
     with the H +  form of a solid cation exchange resin, and allowing the amine or the tetrahydrocarbylammonium hydroxide to react with the cation exchange resin, and thereafter (2) contacting the reacted resin with an aqueous solution of KSb(OH) 6 , 
     wherein each R contains 1-10 C atoms and is independently selected from alkyl, aralkyl and alkylaralkyl, R&#39; is H or H, and wherein x is an indeterminate number of moles of H 2  O.

This invention relates to the preparation of new water-soluble salts ofthe hexahydroantimonate anion, and to such new compounds per se.

In the preparation of catalysts and other Inorganic compositionscontaining antimony, conventional sources of antimony include the oxidesSb₂ 0₃ and Sb₂ 0₄. The oxides are poor sources of antimony due to theirinsolubility and concomitant low reactivity. Another common startingmaterial is the alkali salt, KSb(OH)₆. This salt is moderately solublein hot water, but is often not useful in catalyst preparation because ofthe poisoning effect of potassium in some catalysts, especially at theatom-for-atom level.

It is object of the invention to provide new water-soluble antimony (V)compounds.

It is another object of the invention to provide a novel process formaking such compounds.

Other objects, as well as aspects, features and advantages, of thepresent invention will become apparent from a study of the accompanyingdisclosure and the claims.

These and other objects are realized as a result of the presentinvention according to one aspect of which there is provided a method ofmaking a tri- or tetrahydrocarbylammonium hexahydroxyanimonate,

    [R.sub.3 R'N]Sb(OH).sub.6 ·×H.sub.2 O       (1)

containing 3 to 30 C atoms, which process comprises the steps of (1)contacting a compound selected from

    R.sub.3 N and R.sub.4 and R.sub.4 NOH

with the H⁺ form of a solid cation exchange resin, and allowing theamine or the tetrahydrocarbylammonium hydroxide to react with the cationexchange resin, and thereafter (2) contacting the reacted resin with anaqueous solution of KSb(OH)6,

wherein each R contains 1-10 C atoms and is independently selected fromalkyl, aralkyl and alkylaralkyl, R' is H or R, and wherein x is anindeterminate number of moles of H₂ O.

In the foregoing process, the total C atoms in the compound of formula(1) is usually from 3 to 24, more usually 3 to 18. In the antimonateproducts of formula (1) and in the reactants R₃ N and R₄ NOH, it is mostusual that 3 of the R groups are the same. It is also most usual that 3of the R groups are alkyl, especially containing 1-6 C atoms,particularly 1-4 C atoms.

The new products of the invention of formula (1) are in most instanceswater soluble; even those compounds with the most C atoms that are notwater soluble are water dispersible in the sense that they formemulsions in water because of their ionic nature.

Especially useful products of the invention are those in which 3 of theR groups are C₁ to C₆, particularly C₁ to C₄, alky groups, and R'contains 1-8 C atoms or is H.

In the process of the invention, when the reactant with the cationexchange resin in step (1) is an amine, the resin becomes charged withR₃ NH⁺ ions in step (1). When this reactant is R₄ NOH the cationexchange resin becomes charged with R₄ N⁺ ions and water results fromthe reaction of the H⁺ ion of the resin with the OH⁻ ion from the R₄ NOHreactant. Thereafter, when either charged form of the resin is contactedwith the KSb(OH)₆ solution, the resin becomes charged with K⁺ ions, and,of course, the product [R₃ HN]Sb(OH)₆ or the product R₄ N]Sb(OH)₆,respectively, results.

When compared to KSb(OH)₆, the highly dispersible products of theinvention are much more easily incorporated in aqueous solutions andslurries of inorganic compounds in making inorganic compositions such assolid contact catalysts, ceramics and the like. Of equal importance isthat 5-valent antimony can be introduced without the concomitantintroduction of the potassium ion. Thus, the new counterions, i.e., thetrihydrocarbylammonium or the tetrahydrocarbylammonium cation can beeasily removed from the composition by oxidation or combustion atmoderate calcination temperatures. Finally, the new antimonates of thepresent invention are easily dissolved in polar organic solvents becauseof the new counterions.

In the process of the invention, if it is desired that the new compoundof formula (1) be substantially free of the R₃ N or R₃ R'NOH reactant,the product of step (1) can be washed with water to remove the occludedaqueous solution containing these starting materials before effectingstep (2). For instance, the reacted cation exchange resin from step (1)can be placed in a column and then washed with pure water until theeffluent from the column is essentially free of the amine orhydrocarbylammonium hydroxide, prior to carrying out step (2).

The following examples of the invention are exemplary and should not betaken as in any way limiting.

EXAMPLE 1

Tetra-n-butylammonium hexahydroxyantimonate was made as follows: Acation exchange resin (polystyrene crosslinked with 2% divinylbenzene, Hform, 1.8 meq/ml wet capacity) was charged with Bu₄ N⁺ ions by stirring330 ml resin (0.6 eq) with 55% aqueous tetra-n-butylammonium hydroxidesolution (472 g, 1 eq) for 72 hours (an equal volume of deionized waterwas added for dilution purposes). The flask containing the stirred resinwas sealed in order to prevent reaction of the strongly basic solutionwith atmospheric CO₂. A 250 ml portion of the charged resin was thentransferred to a 300 ml column and washed with deionized water until thepH of the effluent matched the pH of deionized water. A solution ofKSb(OH)₆ (20g) in 1 L of 60°-80° C. deionized water was prepared andcooled to near room temperature. This solution was passed through theresin column at a flow rate of about 1 ml per min. A total volume of3.75 L of KSb(OH)₆ solution (0.275 eq) was passed through the column.The effluent was collected and subsequently rotovapped to dryness (bathtemp <60° C.). A viscous oil was obtained. After drying in vacuo over P₄O₁₀ for 24 hr the oil was converted to an hygroscopic solid.

EXAMPLE 2

Trimethylammonium hexahydroantimonate was prepared as follows:

A cation exchange resin (polystyrene crosslinked with 2% divinylbenzene,H⁺ form, 1.8 meg/g wet capacity) was charged with (H₃ C)₃ NH⁺ ions bystirring 300 ml resin (0.54 eq) with 170g (0.72 eq) of 25 wt% aqueoustrimethylamine solution for 48 hours (200g of deionized water was addedfor dilution purposes). The flask containing the stirred resin wassealed in order to prevent reaction of the strongly basic solution withatmospheric CO ₂. A 150 ml portion of the charged resin was thentransferred to a 300 ml column and washed with deionized water until thepH of the effluent matched the pH of dionized water. A solution ofKSb(OH)₆ (20 g) in 1 L of 60°-80° C. deionized water was prepared andcooled to near room temperature. This solution was passed through theresin column at a flow rate of about 1 ml per min. A total volume of2.5L of KSb(OH)₆ solution was passed through the column. The effluentwas collected and subsequently rotovapped to near dryness (bath temp <60° C.).

EXAMPLE 3

Tetra-n-propylammonium hexahydroantimonate was prepared as follows:

A cation exchange resin (polystyrene crosslinked with 2% divinylbenzene,H form, 1.8 meq/ml wet capacity) was charged with tetra-n-propylammoniumions by stirring 330 ml resin (0.6 eq) with 40% aqueoustetra-n-propylammonium hydroxide solution (350 g) for 72 hours (an equalvolume of deionized water was added for dilution purposes). The flaskcontaining the stirred resin was sealed in order to prevent reaction ofthe strongly basic solution with atmospheric CO₂. A 250 ml portion ofthe charged resin was then transferred to a 300 ml column and washedwith deionized water until the pH of the effluent matched the pH ofdeionized water. A solution of KSb(OH)₆ (20 g) in 1 L of 60°-80° C.deionized water was prepared and cooled to near room temperature. Thissolution was passed through the resin column at a flow rate of about 1ml per min. A total volume of 3.75 L of KSb(OH)₆ solution (0.275 eq) waspassed through the column. The effluent was collected and subsequentlyrotovapped to dryness (bath Temp. <60° C.). A viscous oil was obtained.After drying in vacuo over P₄ O₁₀ for 24 hr the oil was converted to anhygroscopic solid.

EXAMPLE 4

Tetraethylammonium hexahydroantimonate was prepared as follows:

A cation exchange resin (polystyrene crosslinked wIth 2 %divinylbenzene, H form, 1.8 meq/ml wet capacity) was charged withtetraethylammonium ions by stirring 270 ml resin with 40% aqueoustetraethylammonium hydroxide solution (317.5 g) for 72 hours (an equalvolume of deionized water was added for dilution purposes). The flaskcontaining the stirred resin was sealed in order to prevent reaction ofthe strongly basic solution with atmospheric CO₂. A 250 ml portion ofthe resin was then transferred to a 300 ml column and washed withdeionized water until the pH of the effluent matched the pH of deionizedwater. A solution of KSb(OH)₆ (20 g) in 1 L of 60°-80° C. deionizedwater was prepared and cooled to near room temperature. This solutionwas passed through the resin column at a flow rate of about 1 ml permin. A total volume of 3.75 L of KSb(OH)₆ solution (0.275 eq) was passedthrough the column. The effluent was collected and subsequentlyrotovapped to dryness (bath temp< 60° C.). A viscous oil was obtained.After drying in vacuo over P₄ O₁₀ for 24 hr the oil was converted to anhygroscopic solid. The yield was essentially quantitative. The antimonycontent of a dried sample of the [Et₄ N]⁺ salt was determined by aniodometric titrimetic procedure. The average value of a number oftItrations, 32.11% on a weight basis, corresponds to the formula [(CH₃CH₂ )₄ N]Sb(OH)₆.1.4H₂ O (calculated 32.10%).

EXAMPLE 5

Tetramethylammonium hexahydroantimonate was prepared as follows:

A cation exchange resin (polystyrene crosslinked with 2% divinylbenzene,H form, 1.8 meq/ml wet capacity) was charged with tetramethylammonumions by stirring 330 ml resin (0.6 eq) with 6.25% aqueoustetramethylammonium hydroxide solution (1600 g) for 72 hours (an equalvolume of deionized water was added for dilution purposes). The flaskcontaining the stirred resin was sealed in order to prevent reaction ofthe strongly basic solution with atmospheric CO₂. A 250 ml portion ofthe charged resin was then transferred to a 300 ml column and washedwith deionized water until the pH of the effluent matched the pH ofdeionized water. A solution of KSb(OH)₆ (20 g) in 1 L of 60°-80° C.deionized water was prepared and cooled to near room temperature. Thissolution was passed through the resin column at a flow rate of about 1ml per min. A total volume of 3.75 L of KSb(OH)₆ solution (0.275 eq) waspassed through the column. The effluent was collected and subsequentlyrotovapped to dryness (bath temp <60° C.). A viscous oil was obtained.After drying in vacuo over P₄ O₁₀ for 24 hr the oil was converted to anhygroscopic solid.

EXAMPLES 6, 7 and 8

When the procedure of Example 2 was repeated using triethyl-,tri-n-propyl and tri-n-butylamines, instead of trimethyl amine, there isobtained, respectively triethylammonium, tri-n-propylammonium andtri-n-butylammonium hexahydroantimonate.

As noted, the products of the present invention can be used to makecatalyst compositions. An example is as follows:

EXAMPLE 9

9.47 g of [Et₄ N]Sb(OH)₆, as in Example 4, were added to an aqueoussolution of 2.02 g of (VO)SO₄ in 200 ml water, resulting in theimmediate precipitation of a light blue solid. The suspension wasbrought to reflux to dissolve the precipitate. Excess ammonium acetate(2.0g) was then added in order to cause precipitation. The precipitatewas isolated after centrifuging and pouring off the supernatant liquid.In a separate flask, 14.2 g of [Et₄ N]Sb(OH)₆ were dissolved in waterand excess ammonium acetate (11.7g) was added. This also resulted in theformation of a precipitate which was isolated by centrifugation. The twoprecipitates were then resuspended in 200 ml water which contained 2.31g tungstic acid. The water was then removed by evaporative boiling andthe resulting solid was supported on pre-gelled AlOOH SB by thefollowing procedure: The catalyst precursor solids and 11.8g of AlOOH,equivalent to 10.0 g A₂ O₃, were slurried in 40 ml of 10 percent aceticacid solution. This slurry was dried overnight at 110° C. and thenheated 5 hours at 350° C., then crushed and screened to 20-35 mesh and,finally, calcined at 610° C. for 3 hours. Composition: 50%VSb₅ WO_(x+)50% Al₂ O₃.

This catalyst was used to ammoxidize propane over a fixed bed of thecatalyst using molar feed ratios of 1 propane 2.0 NH₃ /3.0 O₂ /6.7 N₂/3.0 H₂ O, using a reactor temperature of 500° C. and a contact time of1.7 secs. Conversion of propane was 75%, and yields were 31%acrylonitrile, 7% propylene and 10% HCN.

As will be evident to those skilled in the art, various modifications ofthis invention can be made or followed in the light of the foregoingdisclosure and discussion without departing from the spirit and scope ofthe disclosure or from the scope of the claims.

We claim:
 1. A new compound, tri- or tetrahydrocarbylammoniumhexahydroxyantimonate, having the formula

    [R.sub.3 R'N]Sb(OH).sub.6·xH.sub.2 O              (1)

wherein each R contains 1-10 C atoms and is independently selected fromalkyl, aralkyl and alkylaralkyl, R' is H or R, and wherein x is anindeterminate number of moles of H₂ O.
 2. A compound of claim 1containing 3 to 24 C atoms.
 3. A compound of claim 1 containing 3 to 18C atoms.
 4. A compound of claim 1 wherein 3 of the R groups are thesame.
 5. A compound of claim 1 wherein R' is is selected from alkyl,aralkyl and alkylaralkyl groups.
 6. A compound of claim 4 wherein R' isR and 3 of the R groups are alkyl groups having 1-6 C atoms.
 7. Acompound of claim 6 wherein the fourth R group contains 1-8 C atoms andis selected from an alkyl, an aralkyl and an alkylaralkyl group.
 8. Acompound

    [R.sub.3 NH]Sb(OH).sub.6 ·xH.sub.2 0

according to claim 1 wherein each R group contains 1-4 C atoms. 9.Trimethylammonium hexahydroantimonate.
 10. A compound of

    [R.sub.4 N]Sb(OH).sub.6 ·xH.sub.2 O

according to claim 11, wherein 3 of the 4 R groups contain 1-4 C atomsand the fourth R group contains 1-8 C atoms.
 11. A compound of claim 11wherein 3 of the 4 R groups are the same.
 12. Tetra-n-butylammoniumhexahydroantimonate.
 13. Tetra-n-propylammonium hexahydroantimonate. 14.Tetraethylammonium hexahydroantimonate.
 15. Tetramethylammoniumhexahydroantimonate.
 16. A compound which is a trihydrocarbylammoniumhexahydroxyantimonate, having the formula

    [R.sub.3 HN]Sb(OH).sub.6 ·xH.sub.2 O              (1)

wherein each R contains 1-10 C atoms and is independently selected fromalkyl, aralkyl and alkylaralkyl, and wherein x is an indeterminatenumber of moles of H₂ O.
 17. A compound of claim 16 containing 3 to 24 Catoms.
 18. A compound of claim 16 containing 3 to 18 C atoms.
 19. Acompound of claim 16 wherein the 3 R groups are the same.
 20. A compoundof claim 19 wherein each of the 3 R groups is an alkyl group having 1-6C atoms.
 21. A compound of claim 5, exclusive of tetramethylammoniumhexahydroxyantimonate.